3-Iodo-1-methyl-1H-pyrazole-4-carboxylic acid

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Reagent Code: #45563
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CAS Number 799835-40-8

science Other reagents with same CAS 799835-40-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.0100 g/mol
Formula C₅H₅IN₂O₂
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MDL Number MFCD28142291
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description Product Description

Used in organic synthesis as a building block for more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of active compounds that target specific biological pathways. Its iodine substituent allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating drug candidates. Additionally, it is employed in research to study enzyme inhibition and receptor binding, aiding in the discovery of new therapeutic agents.

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Test Parameter Specification
Appearance Yellow Solid
Purity (%) 96.5-100%
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,760.00
inventory 1g
10-20 days ฿19,200.00
inventory 5g
10-20 days ฿38,400.00

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3-Iodo-1-methyl-1H-pyrazole-4-carboxylic acid
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Used in organic synthesis as a building block for more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of active compounds that target specific biological pathways. Its iodine substituent allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating drug candidates. Additionally, it is employed in research to study enzyme inhibition and receptor bindin

Used in organic synthesis as a building block for more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of active compounds that target specific biological pathways. Its iodine substituent allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating drug candidates. Additionally, it is employed in research to study enzyme inhibition and receptor binding, aiding in the discovery of new therapeutic agents.

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